124 related articles for article (PubMed ID: 2958791)
1. Use of 4-methylumbelliferyl-6-sulpho-2-acetamido-2-deoxy-beta- D-glucopyranoside for prenatal diagnosis of Tay-Sachs disease using chorionic villi.
Grebner EE; Wenger DA
Prenat Diagn; 1987 Jul; 7(6):419-23. PubMed ID: 2958791
[TBL] [Abstract][Full Text] [Related]
2. First trimester prenatal diagnosis of Tay-Sachs disease using the sulfated synthetic substrate for hexosaminidase A.
Callahan JW; Archibald A; Skomorowski MA; Shuman C; Clarke JT
Clin Biochem; 1990 Dec; 23(6):533-6. PubMed ID: 2149678
[TBL] [Abstract][Full Text] [Related]
3. Usefulness of 4-methylumbelliferyl-6-sulfo-2-acetamido-2-deoxy-beta-D-glucopyrano sid e for the diagnosis of GM2 gangliosidoses in leukocytes.
Inui K; Wenger DA
Clin Genet; 1984 Oct; 26(4):318-21. PubMed ID: 6238730
[TBL] [Abstract][Full Text] [Related]
4. Rapid detection of fetal Mendelian disorders: Tay-Sachs disease.
Guetta E; Peleg L
Methods Mol Biol; 2008; 444():147-59. PubMed ID: 18425478
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis for Tay-Sachs disease using chorionic villus sampling.
Grebner EE; Jackson LG
Prenat Diagn; 1985; 5(5):313-20. PubMed ID: 2933645
[TBL] [Abstract][Full Text] [Related]
6. First-trimester prenatal diagnosis of Tay-Sachs disease.
Grabowski GA; Kruse JR; Goldberg JD; Chockkalingam K; Gordon RE; Blakemore KJ; Mahoney MJ; Desnick RJ
Am J Hum Genet; 1984 Nov; 36(6):1369-78. PubMed ID: 6240199
[TBL] [Abstract][Full Text] [Related]
7. Prenatal Diagnosis of Tay-Sachs Disease.
Zhang J; Chen H; Kornreich R; Yu C
Methods Mol Biol; 2019; 1885():233-250. PubMed ID: 30506202
[TBL] [Abstract][Full Text] [Related]
8. Diagnosis and carrier detection of Tay-Sachs disease: direct determination of hexosaminidase A using 4-methylumbelliferyl derivatives of beta-N-acetylglucosamine-6-sulfate and beta-N-acetylgalactosamine-6-sulfate.
Ben-Yoseph Y; Reid JE; Shapiro B; Nadler HL
Am J Hum Genet; 1985 Jul; 37(4):733-40. PubMed ID: 9556661
[TBL] [Abstract][Full Text] [Related]
9. Tay-Sachs disease heterozygote detection: use of a centrifugal analyser for automation of hexosaminidase assays with two different artificial substrates.
Landels EC; Ellis IH; Bobrow M; Fensom AH
J Med Genet; 1991 Feb; 28(2):101-9. PubMed ID: 1825851
[TBL] [Abstract][Full Text] [Related]
10. Prenatal Tay-Sachs diagnosis by chorionic villi sampling.
Lancet; 1983 Jul; 2(8344):286-7. PubMed ID: 6135112
[No Abstract] [Full Text] [Related]
11. Enzyme studies in GM2 gangliosidiosis, and their application in prenatal diagnosis.
Kaur M; Verma IC
Indian J Pediatr; 1995; 62(4):485-9. PubMed ID: 10829910
[TBL] [Abstract][Full Text] [Related]
12. Detection of Tay-Sachs disease carriers among individuals with thermolabile hexosaminidase B.
Peleg L; Goldman B
Eur J Clin Chem Clin Biochem; 1994 Feb; 32(2):65-9. PubMed ID: 8003579
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of GM2 gangliosidoses using a fluorogenic sulfated substrate.
Inui K; Wenger DA; Furukawa M; Suehara N; Yutaka Y; Okada S; Tanizawa O; Yabuuchi H
Clin Chim Acta; 1986 Jan; 154(2):145-50. PubMed ID: 3955840
[No Abstract] [Full Text] [Related]
14. Synthesis of 4-methylumbelliferyl-beta-D-N-acetylglucosamine-6-sulfate and its use in classification of GM2 gangliosidosis genotypes.
Bayleran J; Hechtman P; Saray W
Clin Chim Acta; 1984 Nov; 143(2):73-89. PubMed ID: 6239713
[TBL] [Abstract][Full Text] [Related]
15. 4-Methylumbelliferyl alpha-N-acetylglucosaminidase activity for diagnosis of Sanfilippo B disease.
Marsh J; Fensom AH
Clin Genet; 1985 Mar; 27(3):258-62. PubMed ID: 3921297
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of GM2 gangliosidosis with high residual hexosaminidase A activity (variant B1; pseudo AB variant).
Conzelmann E; Nehrkorn H; Kytzia HJ; Sandhoff K; Macek M; Lehovský M; Elleder M; Jirásek A; Kobilková J
Pediatr Res; 1985 Nov; 19(11):1220-4. PubMed ID: 2933632
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymograms.
Kustermann-Kuhn B; Harzer K
Hum Genet; 1983; 65(2):172-5. PubMed ID: 6228513
[TBL] [Abstract][Full Text] [Related]
18. In situ assessment of beta-hexosaminidase activity.
Lacorazza HD; Jendoubi M
Biotechniques; 1995 Sep; 19(3):434-40. PubMed ID: 7495557
[TBL] [Abstract][Full Text] [Related]
19. Late onset GM2 gangliosidosis: an alpha-locus genetic compound with near normal hexosaminidase activity.
Charrow J; Inui K; Wenger DA
Clin Genet; 1985 Jan; 27(1):78-84. PubMed ID: 3156697
[TBL] [Abstract][Full Text] [Related]
20. Tay-Sachs disease: one-step assay of beta-N-acetylhexosaminidase in serum with a sulphated chromogenic substrate.
Fuchs W; Navon R; Kaback MM; Kresse H
Clin Chim Acta; 1983 Oct; 133(3):253-61. PubMed ID: 6226458
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]